Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10023335
rs10023335
SHROOM3
1 4 76437834 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10795433
rs10795433
CUBN
1 10 16927924 intron variant A/C snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs11158763
rs11158763 		1 14 68786626 downstream gene variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs112607182
rs112607182 		2 3 170309619 downstream gene variant C/T snv 5.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs12615659
rs12615659 		1 2 186686580 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs1337526
rs1337526 		1 1 47499458 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs147215801
rs147215801
ST8SIA6 ; ST8SIA6-AS1
1 10 17394779 intron variant C/T snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs16940484
rs16940484
TTC39C
1 18 24102336 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs16977473
rs16977473
CGNL1
1 15 57404428 intron variant A/G snv 2.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs17158386
rs17158386 		2 7 29765745 regulatory region variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs2240060
rs2240060
CCHCR1
1 6 31147123 intron variant A/G snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs2470893
rs2470893
CYP1A1
8 0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs2760995
rs2760995
HLA-DRB1
1 6 32606581 intergenic variant G/A snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs28601761
rs28601761 		13 1.000 0.040 8 125487789 intron variant C/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2880119
rs2880119
ACOXL ; MIR4435-2HG
1 2 111051753 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs34071855
rs34071855
CASZ1
4 1 10738432 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3784283
rs3784283
TYRO3
1 15 41575584 intron variant A/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs3795324
rs3795324 		1 1 160673321 non coding transcript exon variant A/C snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs4410790
rs4410790
AHR ; LOC101927609
9 0.882 0.160 7 17244953 intron variant T/C snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs45551835
rs45551835
CUBN
3 1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs4665972
rs4665972
SNX17
9 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs56094641
rs56094641
FTO
4 0.925 0.160 16 53772541 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6535594
rs6535594
NR3C2
2 4 148211605 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs67339103
rs67339103
LRMDA
2 10 76133928 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs677888
rs677888
FBXL20
1 17 39304765 intron variant T/A;G snv 0.29 0.700 1.000 1 2019 2019